Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Sandra Rosas‐Madrigal"'
Autor:
Sandra Romero-Hidalgo, José Flores-Rivera, Verónica Rivas-Alonso, Rodrigo Barquera, María Teresa Villarreal-Molina, Bárbara Antuna-Puente, Luis Rodrigo Macias-Kauffer, Marisela Villalobos-Comparán, Jair Ortiz-Maldonado, Neng Yu, Tatiana V. Lebedeva, Sharon M. Alosco, Juan Daniel García-Rodríguez, Carolina González-Torres, Sandra Rosas-Madrigal, Graciela Ordoñez, Jorge Luis Guerrero-Camacho, Irene Treviño-Frenk, Monica Escamilla-Tilch, Maricela García-Lechuga, Víctor Hugo Tovar-Méndez, Hanna Pacheco-Ubaldo, Victor Acuña-Alonzo, Maria-Cátira Bortolini, Carla Gallo, Gabriel Bedoya, Francisco Rothhammer, Rolando González-Jose, Andrés Ruiz-Linares, Samuel Canizales-Quinteros, Edmond Yunis, Julio Granados, Teresa Corona
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-11 (2020)
Abstract Neuromyelitis Optica (NMO) is an autoimmune disease with a higher prevalence in non-European populations. Because the Mexican population resulted from the admixture between mainly Native American and European populations, we used genome-wide
Externí odkaz:
https://doaj.org/article/e39fd4e23a1a453796fed8b8df762e41
Autor:
Antonia González-Garrido, Sandra Rosas-Madrigal, Arturo Rojo-Domínguez, Jaime Arellanes-Robledo, Enrique López-Mora, Alessandra Carnevale, Leticia Arregui, Rigoberto Rosendo-Gutiérrez, Sandra Romero-Hidalgo, María Teresa Villarreal-Molina
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 21, p 13626 (2022)
The clinical phenotype of LMNA-associated dilated cardiomyopathy (DCM) varies even among individuals who share the same mutation. LMNA encodes lamin AC, which interacts with the lamin-associated protein 2 alpha (LAP2α) encoded by the TMPO gene. The
Externí odkaz:
https://doaj.org/article/48ba0c85ff5f49bd9400874c28b3dc65
Autor:
Sandra Rosas-Madrigal, María Teresa Villarreal-Molina, José Flores-Rivera, Verónica Rivas-Alonso, Luis Rodrigo Macias-Kauffer, Graciela Ordoñez, María del Carmen Chima-Galán, Víctor Acuña-Alonzo, Gastón Macín-Pérez, Rodrigo Barquera, Julio Granados, Ricardo Valle-Rios, Teresa Corona, Alessandra Carnevale, Sandra Romero-Hidalgo
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Neuromyelitis Optica Spectrum Disorder (NMOSD) is a demyelinating autoimmune disease of the central nervous system, more prevalent in individuals of non-European ancestry. Few studies have analyzed genetic risk factors in NMOSD, and HLA class II gene
Externí odkaz:
https://doaj.org/article/aebb55ac4b2e498c8c34592a56d7fbfb
Autor:
Alessandra Carnevale, Sandra Rosas‐Madrigal, Rigoberto Rosendo‐Gutiérrez, Enrique López‐Mora, Sandra Romero‐Hidalgo, Nydia Avila‐Vazzini, Leonor Jacobo‐Albavera, Mayra Domínguez‐Pérez, Gilberto Vargas‐Alarcón, Fernando Pérez‐Villatoro, Juana Inés Navarrete‐Martínez, María Teresa Villarreal–Molina
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 11, Pp n/a-n/a (2020)
Abstract Background Dilated cardiomyopathy (DCM) is a major cause of nonischemic heart failure and death in young adults. Next generation sequencing (NGS) has become part of the diagnostic workup in idiopathic and familial DCM. More than 50 DCM genes
Externí odkaz:
https://doaj.org/article/599d186982a54fa1bc443a52769359ef
Autor:
Bernardo Pérez-Zamorano, Sandra Rosas-Madrigal, Oscar Arturo Migueles Lozano, Manuel Castillo Méndez, Verónica Valverde-Garduño
Publikováno v:
PLoS ONE, Vol 12, Iss 10, p e0186435 (2017)
The innate immune response of Anopheles gambiae involves the transcriptional upregulation of effector genes. Therefore, the cis-regulatory sequences and their cognate binding factors play essential roles in the mosquito's immune response. However, th
Externí odkaz:
https://doaj.org/article/1dc6c27a6819423ab14320bfa47e2f0b
Autor:
Dulce María Moreno-García, Armando Zepeda-Bastida, Juan Ocampo-López, Brisa Rodope Alarcón-Sánchez, Osiris Germán Idelfonso-García, Sandra Rosas-Madrigal, Diana Ivette Aparicio-Bautista, Julio Isael Pérez-Carreón, Saúl Villa-Treviño, Jaime Arellanes-Robledo
Publikováno v:
J Zhejiang Univ Sci B
The online version of the original article can be found athttps://doi.org/10.1631/jzus.B2100201 Erratum to: J Zhejiang Univ-Sci B (Biomed & Biotechnol) 2021 22(12):1045-1052 https://doi.org/10.1631/jzus.B2100201
Autor:
Armando, Zepeda-Bastida, Juan, Ocampo-López, Brisa Rodope, Alarcón-Sánchez, Osiris Germán, Idelfonso-García, Sandra, Rosas-Madrigal, Diana Ivette, Aparicio-Bautista, Julio Isael, Pérez-Carreón, Saúl, Villa-Treviño, Jaime, Arellanes-Robledo
Publikováno v:
J Zhejiang Univ Sci B
Hepatocellular carcinoma (HCC), which is the most frequent primary liver malignancy, is ranked as the sixth most common cancer and the third leading cause of cancer-related deaths worldwide, with its incidence expected to continue rising. One of the
Autor:
Victor Acuña-Alonzo, Alessandra Carnevale, Ricardo Valle-Rios, Verónica Rivas-Alonso, Rodrigo Barquera, Julio Granados, Sandra Rosas-Madrigal, Gastón Macín-Pérez, María del Carmen Chima-Galán, Luis Macías-Kauffer, Sandra Romero-Hidalgo, José Flores-Rivera, Teresa Corona, Graciela Ordoñez, María Teresa Villarreal-Molina
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 12 (2021)
Frontiers in Genetics, Vol 12 (2021)
Neuromyelitis Optica Spectrum Disorder (NMOSD) is a demyelinating autoimmune disease of the central nervous system, more prevalent in individuals of non-European ancestry. Few studies have analyzed genetic risk factors in NMOSD, and HLA class II gene
Autor:
Enrique López-Mora, Hugo Rodríguez-Zanella, Rigoberto Rosendo-Gutiérrez, Ana L. Calderón-Avila, Alessandra Carnevale, Sandra Romero-Hidalgo, Sandra Rosas-Madrigal, María Teresa Villarreal-Molina
Publikováno v:
Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion. 73(5)
espanolAntecedentes: la distrofia muscular congenita de Fukuyama (FCMD) es la forma mas comun de un grupo de trastornos autosomicos recesivos caracterizados por una glicosilacion alterada de a-distroglicanos y causada por mutaciones del gen FKTN. Sin
Autor:
Maricela García-Lechuga, Carla Gallo, Monica Escamilla-Tilch, José Flores-Rivera, Víctor Hugo Tovar-Méndez, María Teresa Villarreal-Molina, Bárbara Antuna-Puente, Verónica Rivas-Alonso, Sandra Romero-Hidalgo, Maria Cátira Bortolini, Tatiana Lebedeva, Juan Daniel García-Rodríguez, Jorge Luis Guerrero-Camacho, Francisco Rothhammer, Hanna Pacheco-Ubaldo, Samuel Canizales-Quinteros, Gabriel Bedoya, Edmond J. Yunis, S. M. Alosco, Victor Acuña-Alonzo, Graciela Ordoñez, Rodrigo Barquera, Luis Macías-Kauffer, Carolina Gonzalez-Torres, Marisela Villalobos-Comparán, Rolando González-José, Julio Granados, Teresa Corona, Sandra Rosas-Madrigal, Neng Yu, Irene Treviño-Frenk, Jair Fernando Ortiz-Maldonado, Andres Ruiz-Linares
Publikováno v:
Scientific Reports
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Scientific Reports, Vol 10, Iss 1, Pp 1-11 (2020)
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Scientific Reports, Vol 10, Iss 1, Pp 1-11 (2020)
Neuromyelitis Optica (NMO) is an autoimmune disease with a higher prevalence in non-European populations. Because the Mexican population resulted from the admixture between mainly Native American and European populations, we used genome-wide microarr